檢索結果 - Rodney C.P. Go
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Kidney Function and Cognitive Impairment in US Adults: The Reasons for Geographic and Racial Differences in Stroke (REGARDS) Study 由 Manjula Kurella Tamura, Virginia G. Wadley, Kristine Yaffe, Leslie A. McClure, George Howard, Rodney C.P. Go, Richard M. Allman, David G. Warnock, William McClellan
出版 2008Revisão -
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Cognitive Status, Stroke Symptom Reports, and Modifiable Risk Factors Among Individuals With No Diagnosis of Stroke or Transient Ischemic Attack in the <i>RE</i> asons for <i>G</i>... 由 Virginia G. Wadley, Leslie A. McClure, Virginia J. Howard, Frederick W. Unverzagt, Rodney C.P. Go, Claudia S. Moy, Martha R. Crowther, Camilo R. Gomez, George Howard
出版 2007Artigo -
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Major histocompatibility complex class III genes and susceptibility to immunoglobulin A deficiency and common variable immunodeficiency. 由 John E. Volanakis, Z B Zhu, Frederick M. Schaffer, Kevin Macon, John Palermos, Bruce O. Barger, Rodney C.P. Go, R. Duncan Campbell, Harry W. Schroeder, Max D. Cooper
出版 1992Artigo -
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Comparison of measures of marker informativeness for ancestry and admixture mapping 由 Lili Ding, Howard W. Wiener, Tilahun Abebe, Mekbib Altaye, Rodney C.P. Go, Carolyn M. Kercsmar, Greg Grabowski, Lisa J. Martin, Gurjit K. Khurana Hershey, Ranajit Chakorborty, Tesfaye M. Baye
出版 2011Artigo -
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Susceptibility Locus for IgA Deficiency and Common Variable Immunodeficiency in the HLA-DR3, -B8, -A1 Haplotypes 由 Harry W. Schroeder, Zeng-Bian Zhu, Ruth March, R. Duncan Campbell, S.M. Berney, Sergei A. Nedospasov, Regina L. Turetskaya, T. Prescott Atkinson, Rodney C.P. Go, Max D. Cooper, John E. Volanakis
出版 1998Artigo -
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A Comprehensive Genetic Association Study of Alzheimer Disease in African Americans 由 Mark W. Logue, Matthew Schu, Badri N. Vardarajan, Jacki Buros, Robert C. Green, Rodney C.P. Go, Patrick Griffith, Thomas O. Obisesan, Rhonna Shatz, Amy R. Borenstein, L. Adrienne Cupples, Kathryn L. Lunetta, M. Daniele Fallin, Clinton T. Baldwin, Lindsay A. Farrer
出版 2011Artigo -
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Project Among African-Americans to Explore Risks for Schizophrenia (PAARTNERS): Evidence for Impairment and Heritability of Neurocognitive Functioning in Families of Schizophrenia... 由 Monica E. Calkins, Ping G. Tepper, Ruben C. Gur, J. Daniel Ragland, Lambertus Klei, Howard W. Wiener, Jan Richard, Robert Savage, Trina B. Allen, Judith O’Jile, Bernie Devlin, Joseph A. Kwentus, Muktar H. Aliyu, L. DiAnne Bradford, Neil B. Edwards, Paul D. Lyons, Vishwajit L. Nimgaonkar, Alberto B. Santos, Rodney C.P. Go, Raquel E. Gur
出版 2010Artigo -
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Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study 由 Carolina Montaño, Margaret A. Taub, Andrew E. Jaffe, Eiríkur Briem, Jason I. Feinberg, Rakel Trygvadottir, Adrian Idrizi, Árni Rafn Rúnarsson, Birna Berndsen, Ruben C. Gur, Tyler M. Moore, Rodney T. Perry, Doug Fugman, Sarven Sabunciyan, Robert H. Yolken, Thomas M. Hyde, Joel E. Kleinman, Janet L. Sobell, Carlos N. Pato, Michele T. Pato, Rodney C.P. Go, Vishwajit L. Nimgaonkar, Daniel R. Weinberger, David Braff, Raquel E. Gur, Margaret Daniele Fallin, Andrew P. Feinberg
出版 2016Artigo -
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Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network 由 Süleyman Gülsüner, Tom Walsh, Amanda C. Watts, Ming K. Lee, Anne Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L. Nimgaonkar, Rodney C.P. Go, Robert Savage, Neal R. Swerdlow, Raquel E. Gur, David Braff, Mary‐Claire King, Jon McClellan, David Braff, Kristin S. Cadenhead, Monica E. Calkins, Dorcas J. Dobie, Robert Freedman, Michael R. Green, Tiffany A. Greenwood, Raquel E. Gur, Ruben C. Gur, Laura C. Lazzeroni, Gregory A. Light, Keith H. Nuechterlein, Ann Olincy, Al Radant, Amrita Ray, Nicholas J. Schork, Larry J. Seidman, Larry J. Siever, Jeremy M. Silverman, William S. Stone, Catherine A. Sugar, Neal R. Swerdlow, Debby W. Tsuang, Ming T. Tsuang, Bruce I. Turetsky, Tolulope Aduroja, Trina B. Allen, Layla Bradford, Monica E. Calkins, Bernie Devlin, Neil B. Edwards, Rohan Ganguli, Rodney C.P. Go, Raquel E. Gur, Ruben C. Gur, Joseph A. Kwentus, Adrienne C. Lahti, Paul D. Lyons, Kim Mathos, Roberta May, S. McLeod-Bryant, Joseph P. McEvoy, Laura Montgomery-Barefield, Vishwajit L. Nimgaonkar, Judith O’Jile, Al Santos, Robert Savage, Charles L. Swanson, William G. Wilson
出版 2013Artigo -
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Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4, and the Risk of Late-Onset Alzheimer Disease in African Americans 由 Christiane Reitz, Gyungah Jun, Adam C. Naj, Ruchita Rajbhandary, Badri N. Vardarajan, Li San Wang, Otto Valladares, Chiao‐Feng Lin, Eric B. Larson, Neill R. Graff‐Radford, Denis A. Evans, Philip L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Jill R. Murrell, Towfique Raj, Nilüfer Ertekin‐Taner, Mark W. Logue, Clinton T. Baldwin, Robert C. Green, Lisa L. Barnes, Laura B. Cantwell, M. Daniele Fallin, Rodney C.P. Go, Patrick Griffith, Thomas O. Obisesan, Jennifer J. Manly, Kathryn L. Lunetta, M. Ilyas Kamboh, Oscar L. López, David A. Bennett, Hugh C. Hendrie, Kathleen Hall, Alison Goate, Goldie S. Byrd, Walter A. Kukull, Tatiana Foroud, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Richard Mayeux
出版 2013Revisão -
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Global and local ancestry in African‐Americans: Implications for Alzheimer's disease risk 由 Timothy J. Hohman, Jessica N. Cooke Bailey, Christiane Reitz, Gyungah Jun, Adam C. Naj, Gary W. Beecham, Zhi Liu, Regina M. Carney, Jeffery M. Vance, Michael L. Cuccaro, Ruchita Rajbhandary, Badri N. Vardarajan, Weixin Wang, Otto Valladares, Chiao‐Feng Lin, Eric B. Larson, Neill R. Graff‐Radford, Denis A. Evans, Philip L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Jill R. Murrell, Towfique Raj, Nilüfer Ertekin‐Taner, Mark W. Logue, Clinton T. Baldwin, Robert C. Green, Lisa L. Barnes, Laura B. Cantwell, M. Daniele Fallin, Rodney C.P. Go, Patrick Griffith, Thomas O. Obisesan, Jennifer J. Manly, Kathryn L. Lunetta, M. Ilyas Kamboh, Oscar L. López, David A. Bennett, John Hardy, Hugh C. Hendrie, Kathleen Hall, Alison Goate, Rosalyn Lang, Goldie S. Byrd, Walter A. Kukull, Tatiana Foroud, Lindsay A. Farrer, Eden R. Martin, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Richard Mayeux, Jonathan L. Haines, Tricia A. Thornton‐Wells
出版 2015Artigo -
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Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel 由 Brian W. Kunkle, Michael A. Schmidt, Hans‐Ulrich Klein, Adam C. Naj, Kara L. Hamilton‐Nelson, Eric B. Larson, Denis A. Evans, Phil L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Nilüfer Ertekin‐Taner, Lisa L. Barnes, M. Daniele Fallin, Jennifer J. Manly, Rodney C.P. Go, Thomas O. Obisesan, M. Ilyas Kamboh, David A. Bennett, Kathleen Hall, Alison Goate, Tatiana M. Foroud, Eden R. Martin, Li‐San Wang, Goldie S. Byrd, Lindsay A. Farrer, Jonathan L. Haines, Gerard D. Schellenberg, Richard Mayeux, Margaret A. Pericak‐Vance, Christiane Reitz, Erin L. Abner, M. Adams Perrie, L. Albin Roger, G Apostolova Liana, Eschrich Steven, S Craig, T. Baldwin Clinton, C. Barber Robert, Sandra Barral, Gunther Thomas, T. James, W. Beecham Gary, H. Bigio Eileen, D. Thomas, Deborah Blacker, F. Boeve Bradley, D. Bowen James, Adam Boxer, R. Burke James, Morris Jeffrey, J Cairns Nigel, Chuanhai Cao, M. Carlsson Cynthia, M. Carney Regina, M. Carrasquillo Minerva, Hugh-Jones David, Carlos Cruchaga, Malcom Dick, Dennis Wilmot, Rachelle S. Doody, Ranjan Duara, M. Faber Kelley, Jaya Thomas, B. Kenneth, W. Fardo David, Roger Martin, Steven H. Ferris, P. Frosch Matthew, R. Galasko Douglas, Marla Gearing, Hervé Daniel, Bernardino Ghetti, John Roshan, C. Green Robert, Harding John, Hákon Hákonarson, L. Hamilton Ronald, John Hardy, E. Harrell Lindy, Steve Lawrence, Mary Ryan, J. Huentelman Matthew, M Hulette Christine, P. Jarvik Gail, Lee‐Way Jin, Anna Karydas, J. Katz Mindy, S. John, C. Dirk Keene, Ronald Kim, H. Kramer Joel, J. Lah James, Yuk Yee Leung, Ge Li, Peter Andrew, B. Richard, G. Lyketsos Constantine, John Malamon, Chammiran Daniel, Frank Martiniuk
出版 2020Revisão -
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Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals 由 Mahdi Ghani, Christiane Reitz, Rong Cheng, Badri N. Vardarajan, Gyungah Jun, Christine Sato, Adam C. Naj, Ruchita Rajbhandary, Li San Wang, Otto Valladares, Chiao‐Feng Lin, Eric B. Larson, Neill R. Graff‐Radford, Denis A. Evans, Philip L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Jill R. Murrell, Towfique Raj, Nilüfer Ertekin‐Taner, Mark Logue, Clinton T. Baldwin, Robert C. Green, Lisa L. Barnes, Laura B. Cantwell, M. Daniele Fallin, Rodney C.P. Go, Patrick Griffith, Thomas O. Obisesan, Jennifer J. Manly, Kathryn L. Lunetta, M. Ilyas Kamboh, Oscar L. López, David A. Bennett, Hugh C. Hendrie, Kathleen Hall, Alison Goate, Goldie S. Byrd, Walter A. Kukull, Tatiana M. Foroud, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Joseph H. Lee, Gerard D. Schellenberg, Peter St George‐Hyslop, Richard Mayeux, Ekaterina Rogaeva, Marilyn Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Robert C. Barber, M. Michael Barmada, Thomas G. Beach, Gary W. Beecham, Duane Beekly, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Guiqing Cai, Nigel J. Cairns, Chuanhai Cao, Chris Carlson, Regina M. Carney, Steven L. Carroll, Helena C. Chui, David G. Clark, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Charles DeCarli, Steven T. DeKosky, F. Yesim Demirci, Malcolm Dick, Kelley M. Faber, Kenneth B. Fallon, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Sid Gilman, Jonathan D. Glass, John H. Growdon, Hakon Hakonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Vahram Haroutunian, Lindy E. Harrell, Lawrence S. Honig, Christine M. Hulette, Bradley T. Hyman
出版 2015Artigo -
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<i>ABCA7</i> frameshift deletion associated with Alzheimer disease in African Americans 由 Holly N. Cukier, Brian W. Kunkle, Badri N. Vardarajan, Sophie Rolati, Kara L. Hamilton‐Nelson, Martin Kohli, Patrice L. Whitehead, Beth A. Dombroski, Derek Van Booven, Rosalyn Lang, Derek M. Dykxhoorn, Lindsay A. Farrer, Michael L. Cuccaro, Jeffery M. Vance, John R. Gilbert, Gary W. Beecham, Eden R. Martin, Regina M. Carney, Richard Mayeux, Gerard D. Schellenberg, Goldie S. Byrd, Jonathan L. Haines, Margaret A. Pericak‐Vance, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Clinton T. Baldwin, M. Michael Barmada, Lisa L. Barnes, Sandra Barral, Thomas G. Beach, James T. Becker, Gary W. Beecham, Duane Beekly, David A. Bennett, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, Adam Boxer, James R. Burke, Jeffrey M. Burns, Joseph D. Buxbaum, Goldie S. Byrd, Guiqing Cai, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Cynthia M. Carlsson, Regina M. Carney, Minerva M. Carrasquillo, Steven L. Carroll, Helena C. Chui, David G. Clark, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Philip L. De Jager, Charles DeCarli, F. Yesim Demirci, Malcolm Dick, Dennis W. Dickson, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley Faber, M. Daniele Fallin, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, Lindsay A. Farrer, Steven H. Ferris, Tatiana Foroud, Matthew P. Frosch, Douglas Galasko, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Rodney C.P. Go, Alison Goate, Neill R. Graff‐Radford, Robert C. Green, Patrick Griffith, John H. Growdon, Jonathan L. Haines, Hákon Hákonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Vahram Haroutunian, Lindy E. Harrell, Lawrence S. Honig, Ryan Huebinger, Christine M. Hulette, Bradley T. Hyman, Gregory A. Jicha, Lee‐Way Jin
出版 2016Artigo
相關主題
Medicine
Biology
Gene
Internal medicine
Genetics
Genotype
Population
Environmental health
Odds ratio
Single-nucleotide polymorphism
Disease
Engineering
Genome-wide association study
Mechanical engineering
Psychiatry
Stroke (engine)
Allele
Cognition
Confidence interval
Demography
Genetic association
Sociology
Allele frequency
Alzheimer's disease
Cohort
Confounding
Gerontology
Physical therapy
Apolipoprotein E
Haplotype